Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
aap Implante AG Recalled by AAP Implantate Ag Due to There is the potential for the Lambotte chisel...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact AAP Implantate Ag directly.
Affected Products
aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended for multiple use.
Quantity: 25 units
Why Was This Recalled?
There is the potential for the Lambotte chisel to break at the welded piece parts of the chisel body and knocking plate.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About AAP Implantate Ag
AAP Implantate Ag has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report